Canonical Allele Identifier: CA413787250
Gene: CHM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.85963958C>A , CM000685.2:g.85963958C>A GRCh38
NC_000023.10:g.85218963C>A , CM000685.1:g.85218963C>A GRCh37
NC_000023.9:g.85105619C>A NCBI36
NG_009874.2:g.88605G>T , LRG_699:g.88605G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357749.7:c.409G>T MANE Select ENSP00000350386.2:p.Ala137Ser
ENST00000357749.6:c.409G>T ENSP00000350386.2:p.Ala137Ser
ENST00000467744.2:n.126+63533G>T
NM_000390.2:c.409G>T , LRG_699t1:c.409G>T NP_000381.1:p.Ala137Ser
XM_006724615.2:c.346G>T XP_006724678.1:p.Ala116Ser
XM_011530839.1:c.-36G>T XP_011529141.1:n.-36G>T
NM_000390.3:c.409G>T NP_000381.1:p.Ala137Ser
NM_001320959.1:c.-36G>T NP_001307888.1:n.-36G>T
NM_001362517.1:c.-36G>T NP_001349446.1:n.-36G>T
NM_001362518.1:c.-36G>T NP_001349447.1:n.-36G>T
NM_001362519.1:c.-36G>T NP_001349448.1:n.-36G>T
XM_017029242.2:c.409G>T XP_016884731.1:p.Ala137Ser
XM_017029246.1:c.-36G>T XP_016884735.1:n.-36G>T
XM_024452331.1:c.-36G>T XP_024308099.1:n.-36G>T
NM_000390.4:c.409G>T MANE Select NP_000381.1:p.Ala137Ser
NM_001362518.2:c.-36G>T NP_001349447.1:n.-36G>T